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Table of Contents
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Summary of Contents for Ossur RHEO KNEE 3
- Page 1 EN | Instructions for Use...
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Page 2: Table Of Contents
SAFETY PRECAUTIONS INDICATIONS FOR USE CONTRAINDICATIONS FOR USE CHARGING THE RHEO KNEE 3 TURNING THE RHEO KNEE 3 ON AND OFF EXTENSION LOCK MAINTENANCE TECHNICAL SPECIFICATIONS... - Page 3 Attention – See instructions for use On / Off Type B Applied Part (IEC60601-1) CE label with Notified Body identification number Non-ionizing radiation Manufacturer Year of manufacture Direct current Consult Instructions for use This marking on the product, packaging, accessories or literature indicates that the product contains electronic components and/ or batteries that should not be disposed of in regular waste at the end of its usable life.
- Page 4 RECOMMENDED FOOT SELECTION Re-Flex Rotate™ Talux Vari-Flex ® ® min = H = Full = – % – = FULL...
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Page 6: Safety Precautions
RHEO KNEE 3 to break down or malfunction, and will void the warranty. 2. If the RHEO KNEE 3 loses power, the knee loses its ability to provide stance support. In such cases it is recommended to manually engage the integrated extension lock to lock the knee in full extension. -
Page 7: Contraindications For Use
To turn the RHEO KNEE 3 on press the ON/OFF button (Figure 4). You will hear a 2 beep confirmation. When the RHEO KNEE 3 is on, you will see a pulsing green light on the light indicator beside the ON/OFF button on the user interface panel. -
Page 8: Technical Specifications
TECHNICAL SPECIFICATIONS Safety standards and classif ication The RHEO KNEE 3 is tested and certified to comply with the IEC/ EN60601-1, standard of electrical safety of medical devices and IEC/ EN60601-1-2, electromagnetic compatibility for medical electrical devices and ISO 10328. - Page 9 EN – Caution: Össur products and components are designed and tested to ISO. Compatibility and compliance with this standard is achieved only when Össur products and components are used with other recommended Össur or authorized components. If un-usual movement or product wear is detected in a structural part of a prosthesis at any time, the patient should be instructed to immediately discontinue use of the device and consult his/her clinical specialist.
- Page 10 Foothill Ranch, CA 92610, USA Miniparc III Tel: +1 (949) 382 3883 Edificio E, Despacho M18 Tel: +1 800 233 6263 28109 El Soto de la Moraleja, ossurusa@ossur.com Alcobendas Madrid – España Össur Canada Tel: 00 800 3539 3668 2150 – 6900 Graybar Road orders.spain@ossur.com...
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